Reaction of large-bite ligands with various tellurium compounds - Synthesis and structural characterization of [Te-2(mu-Cl)(2){(SPPh2)(2)N}(2)], [(4-MeOC6H4TeCl3)(2){mu-Ph2P(S)CH2CH2P(S)P-2}] and [Te-2(mu-Ph2PS2)(2)] representing novel types of tellurium complexes
J. Novosad et al., Reaction of large-bite ligands with various tellurium compounds - Synthesis and structural characterization of [Te-2(mu-Cl)(2){(SPPh2)(2)N}(2)], [(4-MeOC6H4TeCl3)(2){mu-Ph2P(S)CH2CH2P(S)P-2}] and [Te-2(mu-Ph2PS2)(2)] representing novel types of tellurium complexes, POLYHEDRON, 18(22), 1999, pp. 2861-2867
The three title compounds have been synthesized and their structures determ
ined by X-ray crystallography. [Te-2(mu-Cl)(2){(SPPh2)(2)N}(2)], 1, is a di
nuclear square planar Te(II) complex where each Te atom is coordinated to t
he two sulfur atoms of the bidentate dithiolate ligand and to the two bridg
ing chloride ligands. The Te-S bond lengths are 2.4980(8) and 2.5054(8) Ang
strom, while the Te-Cl bond lengths are 2.9065(9) and 2.9230(9) Angstrom. I
n [(4-MeOC6H4TeCl3)(2){mu-Ph2P(S)CH2CH2P(S)Ph-2}], 2, the dithio ligand is
neutral and adds a molecule of [4-MeOC6H4TeCl3] at each sulfur atom, thus b
ridging the two Te(IV) atoms. The coordination of both tellurium atoms is p
si-octahedral with the anisyl group and a lone pair of electrons in axial p
ositions. The Te-S bonds, 2.7747(6) and 2.8198(5) Angstrom, are surprisingl
y weak while the Te-Cl bonds lie in the range 2.4247(5) to 2.5343(6) Angstr
om, those trans to Te-S being shortest. [Te-2(mu-Ph2PS2)(2)], 3, is a binuc
lear Te(I) complex, mainly held together by a Te-Te bond of 2.7298(5) Angst
rom. Both anisobidentate diphenyldithiophosphinate ligands bridge the two t
ellurium atoms. The resulting coordination around each tellurium is best de
scribed as T-shaped with the Te-Te bond along the stem. In the asymmetric n
ear linear S-Te-S system, the short Te-S bonds are 2.487(2) and 2.495(2) An
gstrom while the long bonds are 2.947(2) and 3.033(2) Angstrom, respectivel
y. The strongly different trans influences of the dithio ligands of 1 and 2
are discussed and it is suggested that they are dependent upon the basicit
y of the sulfur atoms. (C) 1999 Elsevier Science Ltd. All rights reserved.